We can do more than simply aspire to a treatment in some undefined future. We are confident that, with your continued support, we will have treatments for FSH muscular dystrophy on the market by the year 2025, so that families everywhere can live out their dreams.
This is a critical time! The patients and families who serve on our Board of Directors have pledged $400,000 for our year-end campaign and challenge you to help match it. Make your donation by midnight December 31st to be counted!
Thank you for making a difference